Canonical Allele Identifier: CA611945927

Gene: NALCN

Linked Data

• dbSNP Id: rs1304048960
• gnomAD v2: 13-101734203-ACTAT-A
• gnomAD v3: 13-101081852-ACTAT-A
• gnomAD v4: 13-101081852-ACTAT-A
• MyVariant Identifiers: chr13:g.101734204_101734207del (hg19) ; chr13:g.101081853_101081856del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081859_101081862del , CM000675.2:g.101081859_101081862del	GRCh38
NC_000013.10:g.101734210_101734213del , CM000675.1:g.101734210_101734213del	GRCh37
NC_000013.9:g.100532211_100532214del	NCBI36
NG_053176.1:g.340351_340354del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3766-210_3766-207del MANE Select	ENSP00000251127.6:n.3766-210_3766-207del
ENST00000648359.1:c.3766-210_3766-207del	ENSP00000497465.1:n.3766-210_3766-207del
ENST00000675150.1:c.3487-210_3487-207del	ENSP00000502680.1:n.3487-210_3487-207del
ENST00000675332.1:c.3853-210_3853-207del	ENSP00000501955.1:n.3853-210_3853-207del
ENST00000676315.1:c.3679-210_3679-207del	ENSP00000501603.1:n.3679-210_3679-207del
ENST00000251127.10:c.3766-210_3766-207del	ENSP00000251127.6:n.3766-210_3766-207del
NM_052867.2:c.3766-210_3766-207del	NP_443099.1:n.3766-210_3766-207del
XM_011521067.1:c.3823-210_3823-207del	XP_011519369.1:n.3823-210_3823-207del
XM_011521068.1:c.3766-210_3766-207del	XP_011519370.1:n.3766-210_3766-207del
XM_011521069.1:c.3736-210_3736-207del	XP_011519371.1:n.3736-210_3736-207del
XM_011521070.1:c.3544-210_3544-207del	XP_011519372.1:n.3544-210_3544-207del
NM_001350748.1:c.3853-210_3853-207del	NP_001337677.1:n.3853-210_3853-207del
NM_001350749.1:c.3766-210_3766-207del	NP_001337678.1:n.3766-210_3766-207del
NM_001350750.1:c.3679-210_3679-207del	NP_001337679.1:n.3679-210_3679-207del
NM_001350751.1:c.3679-210_3679-207del	NP_001337680.1:n.3679-210_3679-207del
NM_052867.3:c.3766-210_3766-207del	NP_443099.1:n.3766-210_3766-207del
XM_011521067.2:c.3823-210_3823-207del	XP_011519369.1:n.3823-210_3823-207del
XM_011521069.2:c.3736-210_3736-207del	XP_011519371.1:n.3736-210_3736-207del
XM_017020536.2:c.3319-210_3319-207del	XP_016876025.1:n.3319-210_3319-207del
XM_017020537.1:c.3001-210_3001-207del	XP_016876026.1:n.3001-210_3001-207del
XM_024449336.1:c.3910-210_3910-207del	XP_024305104.1:n.3910-210_3910-207del
NM_052867.4:c.3766-210_3766-207del MANE Select	NP_443099.1:n.3766-210_3766-207del
NM_001350748.2:c.3853-210_3853-207del	NP_001337677.1:n.3853-210_3853-207del
NM_001350749.2:c.3766-210_3766-207del	NP_001337678.1:n.3766-210_3766-207del
NM_001350750.2:c.3679-210_3679-207del	NP_001337679.1:n.3679-210_3679-207del
NM_001350751.2:c.3679-210_3679-207del	NP_001337680.1:n.3679-210_3679-207del